US5507862A - Anti-fouling compositions or fouling control of harmful aquatic organisms - Google Patents
Anti-fouling compositions or fouling control of harmful aquatic organisms Download PDFInfo
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- US5507862A US5507862A US08/305,922 US30592294A US5507862A US 5507862 A US5507862 A US 5507862A US 30592294 A US30592294 A US 30592294A US 5507862 A US5507862 A US 5507862A
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/45—Heterocyclic compounds having sulfur in the ring
- C08K5/46—Heterocyclic compounds having sulfur in the ring with oxygen or nitrogen in the ring
- C08K5/47—Thiazoles
Definitions
- the present invention relates to fouling control of harmful aquatic organisms which adhere to various water-exposed articles.
- water-exposed articles is used herein to cover marine vessels, buoys, littoral industrial plants, inlet channels for cooling water in thermal or nuclear power stations, drilling rigs for submarine oil fields, harbor facilities and sea pollution preventive bands for ocean civil engineering works, and the like.
- the present inventors have intensively studied to find methods of more effectively preventing and inhibiting various organisms adhering to water-exposed articles.
- harmful aquatic organisms for example, harmful aquatic animals such as barnacles and sea mussels; harmful aquatic plants such as algae and diatoms; and harmful aquatic objects such as slime, thereby completing the present invention.
- the present invention provides a controlling agent and an antifouling coating against harmful aquatic organisms, which comprise an N-phenylbenzoisothiazolone derivative of the formula: ##STR2## wherein R's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; X's are the same or different and are independently halogen, nitro, alkyl or alkoxy; and m is an integer of 0 to 4; with the proviso that when R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all of the R's are different, n is an integer of 2or 3.
- R's are the same or different and are independently halogen, alkyl or alkoxy
- n is an integer of 0 to 5
- X's are the same or different and are independently halogen, nitro, alkyl or alkoxy
- m is an integer of 0 to 4; with the proviso
- the present invention also provides a method for preventing and inhibiting the adhesion of harmful aquatic organisms to water-exposed articles, which comprises applying the antifouling composition of the present invention to the water-exposed articles.
- the controlling agent and antifouling coating of the present invention contain an N-phenylbenzoisothiazolone derivative of the formula (I), which is hereinafter referred to as the compound (I), as an active ingredient.
- Compound (I) is disclosed in the U.S. Pat. No. 3,012,039 and a process of producing this compound is disclosed in the Japanese Patent Publication No. 51-113/1976.
- halogen refers to chlorine, fluorine, bromine or iodine.
- alkyl refers to C 1 -C 10 alkyl such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, tert-butyl, sec-butyl, tert-amyl, n-pentyl, n-hexyl and n-decyl. Preferred is C 1 -C 4 alkyl.
- alkoxy refers to C 1 -C 10 alkoxy such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, tert-amyl oxy, n-pentyloxy, n-hexyloxy and n-decyloxy.
- Preferred is C 1 -C 4 alkoxy.
- the compound (I) has an effect on the prevention and inhibition of harmful aquatic organisms adhering to water-exposed articles, and such an effect can be retained for a long period of time.
- the harmful aquatic organisms are aquatic animals such as barnacles (Balanomorpha), Serpula, polyzoans (Polyzoa), Ascidiacea, Hydrozoa and mollusks (Mollusca); aquatic plants such as Ulva, Enteromorpha, Ectocarpus and diatoms (Diatomaceae); and slime.
- the compound (I) in case where the compound (I) is used for the purpose of preventing and inhibiting the adhesion and propagation of harmful aquatic organisms adhering to water-exposed articles, it may be applied in the form of a solution or emulsion. Preferably, it is applied in the form of a resin-containing composition. In particular, to water-exposed articles present in the sea, the antifouling composition of the present invention is applied.
- the compound (I) can be made into an antifouling composition by ordinary formulation which is usually employed in the field of coatings. It is noted that the compound (I) has no adverse effect on the storage stability, such as viscosity increase and quality change.
- the antifouling composition of the present invention contains the compound (I) in a mixture with a resin.
- the resin are vinyl chloride resins, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl isobutyl ether copolymers, chlorinated rubber resins, chlorinated polyethylene resins, chlorinated polypropylene resins, acrylic resins, styrene-butadiene copolymers, polyester resins, epoxy resins, phenolic resins, synthetic rubbers, silicone rubbers, silicone resins, petroleum resins, oil resins, rosin ester resins, rosin soap and rosin.
- Preferred are vinyl chloride resins, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl isobutyl ether copolymers, acrylic resins and styrene-butadiene copolymers.
- the resin is mixed in an amount of 0.1% to 80% by weight, preferably 0.1% to 60% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention.
- the antifouling composition of the present invention may further contain various additives which are usually used in conventional compositions, for example, plasticizers such as chlorinated paraffin and trimetacresyl phosphate; color pigments such as red iron oxide and titanium dioxide; extender pigments such as zinc oxide and silica powder; and organic solvents such as xylene and methyl isobutyl ketone.
- plasticizers such as chlorinated paraffin and trimetacresyl phosphate
- color pigments such as red iron oxide and titanium dioxide
- extender pigments such as zinc oxide and silica powder
- organic solvents such as xylene and methyl isobutyl ketone.
- a copper compound or a metallic copper is added to the control ling agent and antifouling composition of the present invention to obtain better controlling effects.
- the copper compound are cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate. Preferred are cuprous oxide and copper rhodanide.
- the controlling agent and antifouling composition of the present invention may further contain other conventional antifouling agents, if required.
- the antifouling agent are those which have been cited in the 2091th research meeting of the Japan Shipbuilding Research Association, such as zinc dimethyldithiocarbamate, 2-methylthio-4-t-butylamino-6-cyclopropylamino-s-triazine,2,4,5,6-tetrachloroisophthalonitrile, N,N-dimethyl-N'-(3,4-dichlorophenyl)urea, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, N-(fluorodichloromethylthio)phthalimide, N,N-dimethyl-N'-phenyl-N'-(fluorodichloromethylthio)sulfamide, 2-pyridinethiol-1-oxide zinc salt, tetramethylthiuram disulfide, Cu-10% Ni
- the compound (I) is mixed in an amount of 0.1 to 60% by weight, preferably 0.1 to 40% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention. When the amount is less than 0.1% by weight, no controlling effect will be expected. When the amount is greater than 60% by weight, defects such as cracks and peeling will readily occur on the coating film formed from the antifouling composition.
- the proportion of the copper compound to the compound (I) may vary case by case, but it is preferably in the range of 0.1 to 100 parts by weight to one part by weight of the compound (I).
- the total amount of compound (I) and copper compound is preferably 0.1% to 80% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention. When the total amount is less than 0.1% by weight, no controlling effect will be expected. When the total amount is greater than 80% by weight, defects such as cracks and peeling will readily occur on the coating film formed from the antifouling composition, which makes it difficult to attain the desired antifouling effect.
- the compound (I) can safely be applied as the antifouling composition of the present invention by means of a spray or the like because of its low irritant action.
- LAROFLEX MP-45 vinyl chloride-vinyl isobutyl ether copolymer made by BASF A.G., in Germany
- PLIOLITE S-5B styrene-butadiene copolymer made by The Goodyear Co., in the U.S.A.
- AEROZIL #200 silica powder made by Degsa A.G., in Germany.
- Example 1 Each of the coatings obtained in Examples 1-9 and Comparative Example 1 was applied by means of an air spray to a sandblasted steel panel of 300 ⁇ 100 ⁇ 3.2 mm in size, which had been coated with a shop primer and an anti-corrosive paint of the vinyl tar type, in such a manner that a dry film of 100 ⁇ m in thickness was obtained.
- These sample panels were dried for 7 days, and immersed and left at rest in the sea off the coast of Miyajima in the Bay of Hiroshima at Hiroshima Prefecture, and examined for the adhesion of harmful aquatic animals and plants as well as the adhesion of slime.
- the results are shown in Table 3.
- the amount of adhering harmful aquatic animals and plants in the table was evaluated as the percentage (%) of area to which they adhered, and the amount of adhering slime in the table was evaluated by the following criteria:
- compositions containing the ingredients as shown in Table 4 were obtained in the same manner as employed in Examples 1-9.
- various compositions containing the ingredients as shown in Table 5 were obtained in the same manner.
- compositions obtained in Examples 1-4, 10-13 and Comparative Examples 2-4 were used for the test in which they were actually applied in a patch on to the bottoms of small fishing boats working in three sea areas of Nagasaki Prefecture, Hiroshima Prefecture and Niigata Prefecture. After the lapse of 6 months, the adhesion of harmful aquatic animals and plants as well as the adhesion of slime were evaluated in the same manner as described in Test Example 1. The results are shown in Table 7. The symbol "-" in the table refers to no execution of the test.
- the compound (I) has an excellent effect on the prevention and inhibition of harmful aquatic organisms adhering to water-exposed articles, and such an effect can be retained for a long period of time. Accordingly, the compound (I) can find various applications in the form of a controlling agent or antifouling composition against harmful aquatic organisms.
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Abstract
There are disclosed a controlling agent and an antifouling composition against harmful aquatic organisms, which include a particular N-phenylbenzoisothiazolone derivative of the formula: <IMAGE> (I) wherein R's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; X's are the same or different and are independently halogen, nitro, alkyl or alkoxy; and m is an integer of 0 to 4; with the proviso that when the R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all of the R's are different, n is an integer of 2 or 3. Also disclosed is a method for preventing or inhibiting the adhesion of harmful aquatic organisms to water-exposed articles, which includes applying the antifouling composition to the water-exposed articles.
Description
The present invention relates to fouling control of harmful aquatic organisms which adhere to various water-exposed articles. The term "water-exposed articles" is used herein to cover marine vessels, buoys, littoral industrial plants, inlet channels for cooling water in thermal or nuclear power stations, drilling rigs for submarine oil fields, harbor facilities and sea pollution preventive bands for ocean civil engineering works, and the like.
As there can be found many kinds of animals and plants living in the sea, various organisms may often adhere to water-exposed articles and have adverse effects thereon. The adhesion of such harmful aquatic organisms will cause a decrease in the service speed and an increase in the fuel consumption of marine vessels, and a decrease in the carrying capacity of inlet channels of cooling water.
To control these adhering organisms, various antifouling agents such as cuprous oxide have hitherto been used; however, their efficacy is not sufficient.
Under these circumstances, the present inventors have intensively studied to find methods of more effectively preventing and inhibiting various organisms adhering to water-exposed articles. As a result, they found that particular N-phenylbenzoisothiazolone derivatives have an effect on the prevention and inhibition of adhesion of harmful aquatic organisms, for example, harmful aquatic animals such as barnacles and sea mussels; harmful aquatic plants such as algae and diatoms; and harmful aquatic objects such as slime, thereby completing the present invention.
Thus, the present invention provides a controlling agent and an antifouling coating against harmful aquatic organisms, which comprise an N-phenylbenzoisothiazolone derivative of the formula: ##STR2## wherein R's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; X's are the same or different and are independently halogen, nitro, alkyl or alkoxy; and m is an integer of 0 to 4; with the proviso that when R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all of the R's are different, n is an integer of 2or 3.
The present invention also provides a method for preventing and inhibiting the adhesion of harmful aquatic organisms to water-exposed articles, which comprises applying the antifouling composition of the present invention to the water-exposed articles.
The controlling agent and antifouling coating of the present invention contain an N-phenylbenzoisothiazolone derivative of the formula (I), which is hereinafter referred to as the compound (I), as an active ingredient. Compound (I) is disclosed in the U.S. Pat. No. 3,012,039 and a process of producing this compound is disclosed in the Japanese Patent Publication No. 51-113/1976.
As used herein, the term "halogen" refers to chlorine, fluorine, bromine or iodine. The term "alkyl" refers to C1 -C10 alkyl such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, tert-butyl, sec-butyl, tert-amyl, n-pentyl, n-hexyl and n-decyl. Preferred is C1 -C4 alkyl. The term "alkoxy" refers to C1 -C10 alkoxy such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, tert-amyl oxy, n-pentyloxy, n-hexyloxy and n-decyloxy. Preferred is C1 -C4 alkoxy.
The compound (I) has an effect on the prevention and inhibition of harmful aquatic organisms adhering to water-exposed articles, and such an effect can be retained for a long period of time. Examples of the harmful aquatic organisms are aquatic animals such as barnacles (Balanomorpha), Serpula, polyzoans (Polyzoa), Ascidiacea, Hydrozoa and mollusks (Mollusca); aquatic plants such as Ulva, Enteromorpha, Ectocarpus and diatoms (Diatomaceae); and slime.
In case where the compound (I) is used for the purpose of preventing and inhibiting the adhesion and propagation of harmful aquatic organisms adhering to water-exposed articles, it may be applied in the form of a solution or emulsion. Preferably, it is applied in the form of a resin-containing composition. In particular, to water-exposed articles present in the sea, the antifouling composition of the present invention is applied.
The compound (I) can be made into an antifouling composition by ordinary formulation which is usually employed in the field of coatings. It is noted that the compound (I) has no adverse effect on the storage stability, such as viscosity increase and quality change.
The antifouling composition of the present invention contains the compound (I) in a mixture with a resin. Examples of the resin are vinyl chloride resins, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl isobutyl ether copolymers, chlorinated rubber resins, chlorinated polyethylene resins, chlorinated polypropylene resins, acrylic resins, styrene-butadiene copolymers, polyester resins, epoxy resins, phenolic resins, synthetic rubbers, silicone rubbers, silicone resins, petroleum resins, oil resins, rosin ester resins, rosin soap and rosin. Preferred are vinyl chloride resins, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl isobutyl ether copolymers, acrylic resins and styrene-butadiene copolymers.
The resin is mixed in an amount of 0.1% to 80% by weight, preferably 0.1% to 60% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention.
The antifouling composition of the present invention may further contain various additives which are usually used in conventional compositions, for example, plasticizers such as chlorinated paraffin and trimetacresyl phosphate; color pigments such as red iron oxide and titanium dioxide; extender pigments such as zinc oxide and silica powder; and organic solvents such as xylene and methyl isobutyl ketone.
Preferably, a copper compound or a metallic copper is added to the control ling agent and antifouling composition of the present invention to obtain better controlling effects. Examples of the copper compound are cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate. Preferred are cuprous oxide and copper rhodanide.
The controlling agent and antifouling composition of the present invention may further contain other conventional antifouling agents, if required. Examples of the antifouling agent are those which have been cited in the 2091th research meeting of the Japan Shipbuilding Research Association, such as zinc dimethyldithiocarbamate, 2-methylthio-4-t-butylamino-6-cyclopropylamino-s-triazine,2,4,5,6-tetrachloroisophthalonitrile, N,N-dimethyl-N'-(3,4-dichlorophenyl)urea, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, N-(fluorodichloromethylthio)phthalimide, N,N-dimethyl-N'-phenyl-N'-(fluorodichloromethylthio)sulfamide, 2-pyridinethiol-1-oxide zinc salt, tetramethylthiuram disulfide, Cu-10% Ni solid solution alloy, N-(2,4,6-trichlorophenyl)-maleimide, 2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine, 3-iodo-2-propynylbutyl-carbamate, diiodomethyl-p-tolylsulfone, bisdimethyldithiocarbamoyl zinc ethylenebis-dithiocarbamate and tetraphenylborane pyridine salt.
The compound (I) is mixed in an amount of 0.1 to 60% by weight, preferably 0.1 to 40% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention. When the amount is less than 0.1% by weight, no controlling effect will be expected. When the amount is greater than 60% by weight, defects such as cracks and peeling will readily occur on the coating film formed from the antifouling composition.
In case where a copper compound is to be added to the controlling agent or antifouling composition of the present invention, the proportion of the copper compound to the compound (I) may vary case by case, but it is preferably in the range of 0.1 to 100 parts by weight to one part by weight of the compound (I). The total amount of compound (I) and copper compound is preferably 0.1% to 80% by weight, based on the total weight of the controlling agent or antifouling composition of the present invention. When the total amount is less than 0.1% by weight, no controlling effect will be expected. When the total amount is greater than 80% by weight, defects such as cracks and peeling will readily occur on the coating film formed from the antifouling composition, which makes it difficult to attain the desired antifouling effect.
The compound (I) can safely be applied as the antifouling composition of the present invention by means of a spray or the like because of its low irritant action.
Some typical examples of the compound (I) are shown in Table 1 below, which are to be construed as mere illustrations and not limitations of the preceding disclosure in any way whatsoever.
TABLE 1
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Compound
No. Compound name
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(1) N-phenylbenzoisothiazolone
(2) N-(2-chlorophenyl)benzoisothiazolone
(3) N-(3-chlorophenyl)benzoisothiazolone
(4) N-(4-chlorophenyl)benzoisothiazolone
(5) N-(4-bromophenyl)benzoisothiazolone
(6) N-(2-fluorophenyl)benzoisothiazolone
(7) N-(4-fluorophenyl)benzoisothiazolone
(8) N-(2-methylphenyl)benzoisothiazolone
(9) N-(3-methylphenyl)benzoisothiazolone
(10) N-(4-methylphenyl)benzoisothiazolone
(11) N-(2-ethylphenyl)benzoisothiazolone
(12) N-(3-ethylphenyl)benzoisothiazolone
(13) N-(4-ethylphenyl)benzoisothiazolone
(14) N-(2-isopropylphenyl)benzoisothiazolone
(15) N-(4-isopropylphenyl)benzoisothiazolone
(16) N-(2-methoxyphenyl)benzoisothiazolone
(17) N-(3-methoxyphenyl)benzoisothiazolone
(18) N-(4-methoxyphenyl)benzoisothiazolone
(19) N-(4-ethoxyphenyl)benzoisothiazolone
(20) N-(4-n-butoxyphenyl)benzoisothiazolone
(21) N-(2,4-dichlorophenyl)benzoisothiazolone
(22) N-(3,4-dichlorophenyl)benzoisothiazolone
(23) N-(3,5-dichlorophenyl)benzoisothiazolone
(24) N-(2,6-dichlorophenyl)benzoisothiazolone
(25) N-(2,4,6-trichlorophenyl)benzoisothiazolone
(26) N-(2,3,4,5,6-pentachlorophenyl)benzoisothiazolone
(27) N-(2,4-difluorophenyl)benzoisothiazolone
(28) N-(2,3,5,6-tetrafluorophenyl)benzoisothiazolone
(29) N-(2,3,4,5,6-pentafluorophenyl)benzoisothiazolone
(30) N-(2,4-dimethylphenyl)benzoisothiazolone
(31) N-(3,4-dimethylphenyl)benzoisothiazolone
(32) N-(3,5-dimethylphenyl)benzoisothiazolone
(33) N-(2,6-dimethylphenyl)benzoisothiazolone
(34) N-(2,4,6-trimethylphenyl)benzoisothiazolone
(35) N-(3,4-dimethoxyphenyl)benzoisothiazolone
(36) N-(3,5-dimethoxyphenyl)benzoisothiazolone
(37) N-(3,4,5-trimethoxyphenyl)benzoisothiazolone
(38) N-(2-chloro-4-methylphenyl)benzoisothiazolone
(39) N-(2-fluoro-4-chlorophenyl)benzoisothiazolone
(40) N-(2,6-dichloro-4-methylphenyl)benzoisothiazolone
(41) N-(t-butylphenyl)benzoisothiazolone
(42) N-(2,6-difluorophenyl)benzoisothiazolone
(43) N-(4-iodophenyl)benzoisothiazolone
(44) N-(4-chloro-2-methoxy-5-methylphenyl)benzoisothia-
zolone
(45) N-(2,4-dichloro-3-methylphenyl)benzoisothiazolone
(46) N-(4-ethoxy-3,5-dichlorophenyl)benzoisothiazolone
(47) N-(2-chloro-4-methoxy-3-methylphenyl)benzoisothia-
zolone
(48) N-(4-methoxy-3-chlorophenyl)benzoisothiazolone
(49) N-(3-chloro-2,4-difluorophenyl)benzoisothiazolone
(50) N-(3,4-diethoxyphenyl)benzoisothiazolone
(51) 4-fluoro-N-phenylbenzoisothiazolone
(52) 5-fluoro-N-phenylbenzoisothiazolone
(53) 6-fluoro-N-phenylbenzoisothiazolone
(54) 7-fluoro-N-phenylbenzoisothiazolone
(55) 4-chloro-N-phenylbenzoisothiazolone
(56) 5-chloro-N-phenylbenzoisothiazolone
(57) 6-chloro-N-phenylbenzoisothiazolone
(58) 7-chloro-N-phenylbenzoisothiazolone
(59) 4-bromo-N-phenylbenzoisothiazolone
(60) 5-bromo-N-phenylbenzoisothiazolone
(61) 6-bromo-N-phenylbenzoisothiazolone
(62) 7-bromo-N-phenylbenzoisothiazolone
(63) 6-iodo-N-phenylbenzoisothiazolone
(64) 4-methyl-N-phenylbenzoisothiazolone
(65) 5-methyl-N-phenylbenzoisothiazolone
(66) 6-methyl-N-phenylbenzoisothiazolone
(67) 7-methyl-N-phenylbenzoisothiazolone
(68) 6-ethyl-N-phenylbenzoisothiazolone
(69) 7-propyl-N-phenylbenzoisothiazolone
(70) 4-methoxy-N-phenylbenzoisothiazolone
(71) 5-methoxy-N-phenylbenzoisothiazolone
(72) 6-methoxy-N-phenylbenzoisothiazolone
(73) 7-methoxy-N-phenylbenzoisothiazolone
(74) 5-ethoxy-N-phenylbenzoisothiazolone
(75) 7-isopropoxy-N-phenylbenzoisothiazolone
(76) 4-nitro-N-phenylbenzoisothiazolone
(77) 5-nitro-N-phenylbenzoisothiazolone
(78) 6-nitro-N-phenylbenzoisothiazolone
(79) 7-nitro-N-phenylbenzoisothiazolone
(80) 5,7-dinitro-N-phenylbenzoisothiazolone
(81) 4,5,6,7-tetrafluoro-N-phenylbenzoisothiazolone
(82) 5-chloro-7-fluoro-N-phenylbenzoisothiazolone
(83) 5-methoxy-7-chloro-N-phenylbenzoisothiazolone
(84) 6-chloro-N-(4-chlorophenyl)benzoisothiazolone
(85) 6-chloro-N-(2,3,4-trichlorophenyl)benzoisothiazolone
(86) 5-methyl-N-(3-fluorophenyl)benzoisothiazolone
(87) 6-methoxy-N-(4-chloro-2-methylphenyl)benzoisotia-
zolone
(88) 6-methoxy-N-(2,3,4,5,6-pentachlorophenyl)benzoiso-
thiazolone
(89) 7-methyl-N-(2-methyl-4-chloro-5-methoxyphenyl)-
benzoisothiazolone
(90) 5,7-dimethyl-N-(2-methyl-4-chloro-5-methoxyphenyl)-
benzoisothiazolone
______________________________________
The present invention will be further illustrated by the following examples, test examples and comparative examples, which are not to be construed to limit the scope thereof. Unless otherwise indicated, the term "part(s)" refers to part(s) by weight. Specific examples of the compound (I) are designated by the respective compound numbers shown in Table 1.
To each of the compound (1), (4), (8), (16), (57), (67), (72) and (80) were added the ingredients as shown in Table 2. These mixtures were independently mixed and dispersed with a paint conditioner, which afforded compositions of Examples 1-9. In the same manner, a composition of Comparative Example 1 was obtained. The trade names of the ingredients used are as follows:
LAROFLEX MP-45: vinyl chloride-vinyl isobutyl ether copolymer made by BASF A.G., in Germany
PLIOLITE S-5B: styrene-butadiene copolymer made by The Goodyear Co., in the U.S.A.
AEROZIL #200: silica powder made by Degsa A.G., in Germany.
TABLE 2
__________________________________________________________________________
Examples Comparative
1 2 3 4 5 6 7 8 9 Example
__________________________________________________________________________
1
Compound (1)
30 30
Compound (16) 30
Compound (4) 30
Compound (8) 30
Compound (57) 30
Compound (67) 30
Compound (72) 30
Compound (80) 30
LAROFLEX MP-45
10 10 10 10 10 10 10 10 10
PLIOLITE S-5B 10
Copper rhodanide 30
Red iron oxide
5 5 5 5 5 5 5 5 5 5
Zinc oxide 5 5 5 5 5 5 5 5 5 5
AEROZIL #200
1 1 1 1 1 1 1 1 1 1
Chlorinated paraffin
2 2 2 2 2 2 2 2 2 2
Rosin 10 10 10 10 10 10 10 10 10 10
Xylene 32 32 32 32 32 32 32 32 32 32
Methyl isobutyl ketone
5 5 5 5 5 5 5 5 5 5
Total 100 100 100 100 100 100 100 100 100 100
__________________________________________________________________________
Each of the coatings obtained in Examples 1-9 and Comparative Example 1 was applied by means of an air spray to a sandblasted steel panel of 300×100×3.2 mm in size, which had been coated with a shop primer and an anti-corrosive paint of the vinyl tar type, in such a manner that a dry film of 100 μm in thickness was obtained. These sample panels were dried for 7 days, and immersed and left at rest in the sea off the coast of Miyajima in the Bay of Hiroshima at Hiroshima Prefecture, and examined for the adhesion of harmful aquatic animals and plants as well as the adhesion of slime. The results are shown in Table 3. The amount of adhering harmful aquatic animals and plants in the table was evaluated as the percentage (%) of area to which they adhered, and the amount of adhering slime in the table was evaluated by the following criteria:
0: no adhesion; 1: slight adhesion; 2: small adhesion; 3: moderate adhesion; 4: moderate to great adhesion; and 5: great adhesion.
TABLE 3
__________________________________________________________________________
6 months 12 months 18 months
Immersion Harmful Harmful Harmful
period aquatic aquatic aquatic
Adhering animals animals animals
objects
Slime
and plants
Slime
and plants
Slime
and plants
__________________________________________________________________________
Example 1
0 0 1 0 2 0
Example 2
1 0 2 5 2 5
Example 3
2 0 2 5 3 15
Example 4
0 0 1 5 1 10
Example 5
1 0 1 0 2 0
Example 6
2 0 2 10 3 30
Example 7
1 0 2 5 2 15
Example 8
0 0 1 0 1 5
Example 9
1 0 1 5 2 5
Comparative
5 10 5 60 5 100
Example 1
__________________________________________________________________________
Various compositions containing the ingredients as shown in Table 4 were obtained in the same manner as employed in Examples 1-9. For comparison, various compositions containing the ingredients as shown in Table 5 were obtained in the same manner.
TABLE 4
__________________________________________________________________________
Examples
10 11 12 13 14 15 16 17 18
__________________________________________________________________________
Compound (1) 5
Compound (16) 5
Compound (4) 5
Compound (8) 5 5
Compound (57) 5
Compound (67) 5
Compound (72) 5
Compound (80) 5
LAROFLEX MP-45 10 10 10 10 10 10 10
PLIOLITE S-5B 10 10
Cuprous oxide 30 30 20 20 20 30 30 30 30
Zinc dimethyldithiocarbamate
5
2,4,5,6-Tetrachloroisophthalonitrile
5
N,N-dimethyl-N'-(3,4-dichlorophenyl)urea
5
Red iron oxide 5 5 5 5 5 5 5 5 5
Zinc oxide 5 5 5 5 5 5 5 5 5
AEROZIL #200 1 1 1 1 1 1 1 1 1
Chlorinated paraffin
2 2 2 2 2 2 2 2 2
Rosin 10 10 10 10 10 10 10 10 10
Xylene 27 27 32 32 32 27 27 27 27
Methyl isobutyl ketone
5 5 5 5 5 5 5 5 5
TOTAL 100 100 100 100 100 100 100 100 100
__________________________________________________________________________
TABLE 5
______________________________________
Comparative Examples
2 3 4
______________________________________
LAROFLEX MP-45 10
PLIOLITE S-5B 10 10
Cuprous oxide 30 30
copper rhodanide 20
Zinc dimethyldithiocarbamate 10
Red iron oxide 5 5 5
Zinc oxide 5 5 5
AEROZIL #200 1 1 1
Chlorinated paraffin
2 2 2
Rosin 10 10 10
Xylene 32 32 32
Methyl isobutyl ketone
5 5 5
Total 100 100 100
______________________________________
The compositions obtained in Examples 10-18 and Comparative Examples 1-4 were examined in the same method as used in Test Example 1. The results are shown in Table 6.
TABLE 6
__________________________________________________________________________
6 months 12 months 18 months
Immersion Harmful Harmful Harmful
period aquatic aquatic aquatic
Adhering animals animals animals
objects
Slime
and plants
Slime
and plants
Slime
and plants
__________________________________________________________________________
Example 10
1 0 1 0 2 0
Example 11
1 0 1 0 2 0
Example 12
2 0 3 0 3 5
Example 13
1 0 2 0 2 0
Example 14
0 0 1 0 2 0
Example 15
2 0 3 0 3 10
Example 16
1 0 2 0 2 0
Example 17
0 0 1 0 2 0
Example 18
1 0 1 0 2 0
Comp. Ex. 1
5 10 5 60 5 100
Comp. Ex. 2
5 0 5 10 5 30
Comp. Ex. 3
5 0 5 10 5 30
Comp. Ex. 4
3 0 5 30 5 60
__________________________________________________________________________
The compositions obtained in Examples 1-4, 10-13 and Comparative Examples 2-4 were used for the test in which they were actually applied in a patch on to the bottoms of small fishing boats working in three sea areas of Nagasaki Prefecture, Hiroshima Prefecture and Niigata Prefecture. After the lapse of 6 months, the adhesion of harmful aquatic animals and plants as well as the adhesion of slime were evaluated in the same manner as described in Test Example 1. The results are shown in Table 7. The symbol "-" in the table refers to no execution of the test.
TABLE 7
__________________________________________________________________________
Nagasaki Hiroshima Niigata
Immersion Harmful Harmful Harmful
place aquatic aquatic aquatic
Adhering animals animals animals
objects
Slime
and plants
Slime
and plants
Slime
and plants
__________________________________________________________________________
Example 1
-- -- 0 0 0 0
Example 2
-- -- 0 0 0 0
Example 3
-- -- 1 0 0 0
Example 4
-- -- 0 0 0 0
Example 10
0 0 0 0 -- --
Example 11
0 0 1 0 -- --
Example 12
1 0 2 0 -- --
Example 13
0 0 0 0 -- --
Comp. Ex. 2
5 0 5 0 5 0
Comp. Ex. 4
-- -- 5 10 4 5
__________________________________________________________________________
As described above, the compound (I) has an excellent effect on the prevention and inhibition of harmful aquatic organisms adhering to water-exposed articles, and such an effect can be retained for a long period of time. Accordingly, the compound (I) can find various applications in the form of a controlling agent or antifouling composition against harmful aquatic organisms.
Claims (27)
1. An aquatic anti-fouling composition which comprises an effective anti-fouling amount of N-phenylbenzoisothiazolone derivative of the formula: ##STR3## wherein R's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; X's are the same or different and are independently halogen, nitro, alkyl or alkoxy; and m is an integer of 0 to 4; with the proviso that when R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all of the R's are different, n is an integer of 2 or 3; and a copper material selected from the group consisting of a copper compound and metallic copper, present in an amount of from 0.1 to 100 parts by weight to one part of said N-phenylbenzoisothiazolone derivative.
2. An aquatic anti-fouling composition according to claim 1, wherein the R's are the same or different and are independently halogen, C1 -C10 alkyl or C1 -C10 alkoxy; and the m is an integer of 0.
3. An aquatic anti-fouling composition according to claim 1, wherein the n is an integer of 0 and the m is an integer of 0.
4. An aquatic anti-fouling composition according to claim 1, wherein said copper compound is a member selected from the group consisting of cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate.
5. An aquatic anti-fouling composition according to claim 4, wherein the copper compound is cuprous oxide.
6. A composition according to claim 1, wherein:
said N-phenylbenzoisothiazolone derivative is present in an amount between 0.1% and 60% by weight, based on the total weight of the anti-fouling composition; and
said copper material is present in an amount of from 0.1 to 100 parts by weight to one part of said N-phenylbenzoisothiazolone derivative.
7. An anti-fouling composition against harmful aquatic organisms, which comprises an effective anti-fouling amount of an N-phenylbenzoisothiazolone derivative of the formula: ##STR4## wherein R's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; X's are the same or different and are independently halogen, nitro, alkyl or alkoxy; and m is an integer of 0 to 4; with the proviso that when R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all the R's are different, n is an integer of 2 or 3, and a resin.
8. An anti-fouling composition according to claim 7, wherein the R's are the same or different and are independently halogen, C1 -C10 alkyl or C1 -C10 alkoxy; and the m is an integer of 0.
9. An anti-fouling composition according to claim 7, wherein the n is an integer of 0 and the m is an integer of 0.
10. An anti-fouling composition according to claim 7, which further comprises a copper material selected from the group consisting of a copper compound and metallic copper.
11. An anti-fouling composition according to claim 8, which further comprises a copper material selected from the group consisting of a copper compound and metallic copper.
12. An anti-fouling composition according to claim 9, which further comprises a copper material selected from the group consisting of a copper compound and metallic copper.
13. An anti-fouling composition according to claim 7, which further comprises metallic copper or a copper compound selected from the group consisting of cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate.
14. An anti-fouling composition according to claim 8, which further comprises metallic copper or a copper compound selected from the group consisting of cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate.
15. An anti-fouling composition according to claim 9, which further comprises metallic copper or a copper compound selected from the group consisting of cuprous oxide, copper rhodanide, oxine-copper, copper naphthenate, copper glycinate, cuprous chloride and cuprous carbonate copper.
16. An anti-fouling composition according to claim 13, wherein the copper compound is cuprous oxide.
17. An anti-fouling composition according to claim 14, wherein the copper compound is cuprous oxide.
18. An anti-fouling composition according to claim 15, wherein the copper compound is cuprous oxide.
19. An anti-fouling composition according to any one of claims 7-18, wherein the resin is selected from the group consisting of vinyl chloride resins, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl isobutyl ether copolymers, chlorinated rubber resins, chlorinated polyethylene resins, chlorinated polypropylene resins, acrylic resins, styrene-butadiene copolymers, polyester resins, epoxy resins, phenolic resins, synthetic rubbers, silicone rubbers, silicone resins, petroleum resins, oil resins, rosin ester resins, rosin soap and rosin.
20. A composition according to claim 7, wherein:
said N-phenylbenzoisothiazolone derivative is present in an amount between 0.1% and 60% by weight, based on the total weight of the anti-fouling composition; and
said resin is present in an amount between 0.1% and 80% by weight based on the total weight of the composition.
21. A composition according to claim 20, which further comprises a copper material selected from the group consisting of a copper compound and metallic copper, present in an amount of from 0.1 to 100 parts by weight to one part of said N-phenylbenzoisothiazolone derivative.
22. A method for preventing or inhibiting the adhesion of harmful aquatic organisms to a water-exposed article, which comprises applying an effective anti-fouling amount of the anti-fouling composition according to claim 7 to the water-exposed article.
23. A method according to claim 22, wherein the water-exposed article is present in the sea.
24. A method according to claim 23, wherein the water-exposed article is a marine vessel.
25. A method for preventing or inhibiting the adhesion of harmful aquatic organisms to a water-exposed article, which comprises applying an effective anti-fouling amount of an anti- fouling composition containing N-phenylbenzoisothiazolone to a water-exposed article.
26. A method for preventing or inhibiting the adhesion of harmful aquatic organisms to a water-exposed article which comprises applying an effective anti-fouling amount of an anti-fouling composition containing an N-phenylbenzoisothiazolone derivative of the general formula: ##STR5## wherein R's are the same or different and are independently halogen, C1 -C10 alkyl or C1 -C10 alkoxy; X's are the same or different and are independently halogen, alkyl or alkoxy; n is an integer of 0 to 5; and m is an integer of 0 with the proviso that when R's are all alkyl or all alkoxy, n is an integer of 1 to 3, and when all the R's are different, n is an integer of 2 or 3, and a resin.
27. A method according to claim 26, wherein the n is an integer of 0.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23137393 | 1993-09-17 | ||
| JP33379293 | 1993-12-27 | ||
| JP5-231373 | 1993-12-27 | ||
| JP5-333792 | 1993-12-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5507862A true US5507862A (en) | 1996-04-16 |
Family
ID=26529827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/305,922 Expired - Fee Related US5507862A (en) | 1993-09-17 | 1994-09-16 | Anti-fouling compositions or fouling control of harmful aquatic organisms |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5507862A (en) |
| EP (1) | EP0644243B1 (en) |
| KR (1) | KR950007665A (en) |
| CN (1) | CN1103544A (en) |
| DE (1) | DE69416221T2 (en) |
| ES (1) | ES2129559T3 (en) |
| GR (1) | GR3029832T3 (en) |
| IT (1) | IT1267458B1 (en) |
| SG (1) | SG70550A1 (en) |
| TW (1) | TW385231B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6692557B1 (en) * | 1997-07-24 | 2004-02-17 | Unisearch Limited | Antifouling of shellfish and aquaculture apparatus |
| US20060021546A1 (en) * | 2004-07-23 | 2006-02-02 | Xerox Corporation | Processes for preparing phase change inks |
| US20060142587A1 (en) * | 2004-11-08 | 2006-06-29 | L'oreal | Benzoisothiazolone compositions |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102234251B (en) * | 2010-04-20 | 2013-04-24 | 中国科学院烟台海岸带研究所 | Benzisothiazolinone compound and application thereof |
| CN105238149A (en) * | 2015-09-22 | 2016-01-13 | 安徽皖东化工有限公司 | Nanometer titanium carbide-nanometer silver composite marine coating and manufacturing method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012039A (en) * | 1958-03-14 | 1961-12-05 | Ici Ltd | 2-p-chlorobenzyl-1, 2-benzisothiazolone |
| DE2439619A1 (en) * | 1973-08-20 | 1975-02-27 | Rohm & Haas | COATING DIMENSIONS |
| JPS51113A (en) * | 1974-06-19 | 1976-01-05 | Kitagawa Iron Works Co | Nanjakujibanno kokakoho |
| US4243403A (en) * | 1967-03-09 | 1981-01-06 | Rohm And Haas Company | 3-Isothiazolones |
| US4822511A (en) * | 1988-05-06 | 1989-04-18 | Rohm And Haas Company | Preservative compositions comprising a synergistic mixture of isothiagolones |
| US5108500A (en) * | 1990-12-10 | 1992-04-28 | Rohm And Haas Company | Stabilization of water insoluble 3-isothiazolones |
| US5125967A (en) * | 1989-03-31 | 1992-06-30 | Imperial Chemical Industries Plc | Biocidal composition comprising an isothiazolinone derivative and a substituted urea or halogenated aromatic alkyl sulphoxide or sulphone |
| US5188663A (en) * | 1990-09-14 | 1993-02-23 | Rohm And Haas Company | Aquatic antifouling composition |
| US5364874A (en) * | 1990-04-27 | 1994-11-15 | Zeneca Limited | Biocide composition and use |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE392103B (en) * | 1970-04-27 | 1977-03-14 | Sherwin Williams Co | METHOD OF PRODUCING 1,2-BENSISOTIAZOLINE-3-ONERS |
| JPS50142701A (en) * | 1974-05-02 | 1975-11-17 | ||
| US4127687A (en) * | 1976-07-19 | 1978-11-28 | Rohm And Haas Company | Prevention of fouling of marine structures such as boat hulls |
| GB9003871D0 (en) * | 1990-02-21 | 1990-04-18 | Rohm & Haas | Stabilization of isothiazolones |
-
1994
- 1994-09-14 TW TW083108462A patent/TW385231B/en active
- 1994-09-15 KR KR1019940023454A patent/KR950007665A/en not_active Ceased
- 1994-09-16 EP EP94114600A patent/EP0644243B1/en not_active Expired - Lifetime
- 1994-09-16 CN CN94115922A patent/CN1103544A/en active Pending
- 1994-09-16 US US08/305,922 patent/US5507862A/en not_active Expired - Fee Related
- 1994-09-16 DE DE69416221T patent/DE69416221T2/en not_active Expired - Fee Related
- 1994-09-16 SG SG1996000918A patent/SG70550A1/en unknown
- 1994-09-16 ES ES94114600T patent/ES2129559T3/en not_active Expired - Lifetime
- 1994-09-16 IT IT94TO000723A patent/IT1267458B1/en active IP Right Grant
-
1999
- 1999-03-31 GR GR990400923T patent/GR3029832T3/en unknown
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012039A (en) * | 1958-03-14 | 1961-12-05 | Ici Ltd | 2-p-chlorobenzyl-1, 2-benzisothiazolone |
| US4243403A (en) * | 1967-03-09 | 1981-01-06 | Rohm And Haas Company | 3-Isothiazolones |
| DE2439619A1 (en) * | 1973-08-20 | 1975-02-27 | Rohm & Haas | COATING DIMENSIONS |
| JPS51113A (en) * | 1974-06-19 | 1976-01-05 | Kitagawa Iron Works Co | Nanjakujibanno kokakoho |
| US4822511A (en) * | 1988-05-06 | 1989-04-18 | Rohm And Haas Company | Preservative compositions comprising a synergistic mixture of isothiagolones |
| US5125967A (en) * | 1989-03-31 | 1992-06-30 | Imperial Chemical Industries Plc | Biocidal composition comprising an isothiazolinone derivative and a substituted urea or halogenated aromatic alkyl sulphoxide or sulphone |
| US5364874A (en) * | 1990-04-27 | 1994-11-15 | Zeneca Limited | Biocide composition and use |
| US5188663A (en) * | 1990-09-14 | 1993-02-23 | Rohm And Haas Company | Aquatic antifouling composition |
| US5108500A (en) * | 1990-12-10 | 1992-04-28 | Rohm And Haas Company | Stabilization of water insoluble 3-isothiazolones |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6692557B1 (en) * | 1997-07-24 | 2004-02-17 | Unisearch Limited | Antifouling of shellfish and aquaculture apparatus |
| US20060021546A1 (en) * | 2004-07-23 | 2006-02-02 | Xerox Corporation | Processes for preparing phase change inks |
| US20060142587A1 (en) * | 2004-11-08 | 2006-06-29 | L'oreal | Benzoisothiazolone compositions |
| US7232839B2 (en) * | 2004-11-08 | 2007-06-19 | L'oreal | Benzoisothiazolone compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| TW385231B (en) | 2000-03-21 |
| KR950007665A (en) | 1995-04-15 |
| DE69416221D1 (en) | 1999-03-11 |
| EP0644243A3 (en) | 1996-01-10 |
| IT1267458B1 (en) | 1997-02-05 |
| CN1103544A (en) | 1995-06-14 |
| EP0644243A2 (en) | 1995-03-22 |
| GR3029832T3 (en) | 1999-06-30 |
| SG70550A1 (en) | 2000-02-22 |
| EP0644243B1 (en) | 1999-01-27 |
| ITTO940723A1 (en) | 1996-03-16 |
| ITTO940723A0 (en) | 1994-09-16 |
| ES2129559T3 (en) | 1999-06-16 |
| DE69416221T2 (en) | 1999-10-14 |
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Legal Events
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Owner name: CHUGOKU MARINE PAINTS, LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TSUBOI, MAKOTO;YUKI, SHUHEI;ARAI, KENJI;AND OTHERS;REEL/FRAME:007222/0313;SIGNING DATES FROM 19940929 TO 19941013 Owner name: SUMITOMO CHEMICAL COMPANY LIMITED, JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TSUBOI, MAKOTO;YUKI, SHUHEI;ARAI, KENJI;AND OTHERS;REEL/FRAME:007222/0313;SIGNING DATES FROM 19940929 TO 19941013 |
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